Cargando…

Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling

The linker of nucleoskeleton and cytoskeleton (LINC) complex is a protein complex spanning the inner and outer membranes of the nuclear envelope. Outer nuclear membrane KASH proteins interact in the nuclear envelope lumen with inner nuclear membrane SUN proteins. The paralogous Arabidopsis KASH prot...

Descripción completa

Detalles Bibliográficos
Autores principales: Biel, Alecia, Moser, Morgan, Groves, Norman R., Meier, Iris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120628/
https://www.ncbi.nlm.nih.gov/pubmed/35599883
http://dx.doi.org/10.3389/fpls.2022.784342
_version_ 1784710970851983360
author Biel, Alecia
Moser, Morgan
Groves, Norman R.
Meier, Iris
author_facet Biel, Alecia
Moser, Morgan
Groves, Norman R.
Meier, Iris
author_sort Biel, Alecia
collection PubMed
description The linker of nucleoskeleton and cytoskeleton (LINC) complex is a protein complex spanning the inner and outer membranes of the nuclear envelope. Outer nuclear membrane KASH proteins interact in the nuclear envelope lumen with inner nuclear membrane SUN proteins. The paralogous Arabidopsis KASH proteins SINE1 and SINE2 function during stomatal dynamics induced by light–dark transitions and ABA. Previous studies have shown F-actin organization, cytoplasmic calcium (Ca(2+)) oscillations, and vacuolar morphology changes are involved in ABA-induced stomatal closure. Here, we show that SINE1 and SINE2 are both required for actin pattern changes during ABA-induced stomatal closure, but influence different, temporally distinguishable steps. External Ca(2+) partially overrides the mutant defects. ABA-induced cytoplasmic Ca(2+) oscillations are diminished in sine2-1 but not sine1-1, and this defect can be rescued by both exogenous Ca(2+) and F-actin depolymerization. We show first evidence for nuclear Ca(2+) oscillations during ABA-induced stomatal closure, which are disrupted in sine2-1. Vacuolar fragmentation is impaired in both mutants and is partially rescued by F-actin depolymerization. Together, these data indicate distinct roles for SINE1 and SINE2 upstream of this network of players involved in ABA-based stomatal closure, suggesting a role for the nuclear surface in guard cell ABA signaling.
format Online
Article
Text
id pubmed-9120628
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-91206282022-05-21 Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling Biel, Alecia Moser, Morgan Groves, Norman R. Meier, Iris Front Plant Sci Plant Science The linker of nucleoskeleton and cytoskeleton (LINC) complex is a protein complex spanning the inner and outer membranes of the nuclear envelope. Outer nuclear membrane KASH proteins interact in the nuclear envelope lumen with inner nuclear membrane SUN proteins. The paralogous Arabidopsis KASH proteins SINE1 and SINE2 function during stomatal dynamics induced by light–dark transitions and ABA. Previous studies have shown F-actin organization, cytoplasmic calcium (Ca(2+)) oscillations, and vacuolar morphology changes are involved in ABA-induced stomatal closure. Here, we show that SINE1 and SINE2 are both required for actin pattern changes during ABA-induced stomatal closure, but influence different, temporally distinguishable steps. External Ca(2+) partially overrides the mutant defects. ABA-induced cytoplasmic Ca(2+) oscillations are diminished in sine2-1 but not sine1-1, and this defect can be rescued by both exogenous Ca(2+) and F-actin depolymerization. We show first evidence for nuclear Ca(2+) oscillations during ABA-induced stomatal closure, which are disrupted in sine2-1. Vacuolar fragmentation is impaired in both mutants and is partially rescued by F-actin depolymerization. Together, these data indicate distinct roles for SINE1 and SINE2 upstream of this network of players involved in ABA-based stomatal closure, suggesting a role for the nuclear surface in guard cell ABA signaling. Frontiers Media S.A. 2022-05-06 /pmc/articles/PMC9120628/ /pubmed/35599883 http://dx.doi.org/10.3389/fpls.2022.784342 Text en Copyright © 2022 Biel, Moser, Groves and Meier. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Biel, Alecia
Moser, Morgan
Groves, Norman R.
Meier, Iris
Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling
title Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling
title_full Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling
title_fullStr Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling
title_full_unstemmed Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling
title_short Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling
title_sort distinct roles for kash proteins sine1 and sine2 in guard cell actin reorganization, calcium oscillations, and vacuolar remodeling
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120628/
https://www.ncbi.nlm.nih.gov/pubmed/35599883
http://dx.doi.org/10.3389/fpls.2022.784342
work_keys_str_mv AT bielalecia distinctrolesforkashproteinssine1andsine2inguardcellactinreorganizationcalciumoscillationsandvacuolarremodeling
AT mosermorgan distinctrolesforkashproteinssine1andsine2inguardcellactinreorganizationcalciumoscillationsandvacuolarremodeling
AT grovesnormanr distinctrolesforkashproteinssine1andsine2inguardcellactinreorganizationcalciumoscillationsandvacuolarremodeling
AT meieriris distinctrolesforkashproteinssine1andsine2inguardcellactinreorganizationcalciumoscillationsandvacuolarremodeling